美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA214982"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
50090-6708-1 50090-6708 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20230928 N/A ANDA ANDA214982 A-S Medication Solutions DIGOXIN .125 mg/1 100 TABLET in 1 BOTTLE (50090-6708-1)
59651-437-01 59651-437 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20220208 N/A ANDA ANDA214982 Aurobindo Pharma Limited DIGOXIN .125 mg/1 100 TABLET in 1 BOTTLE (59651-437-01)
59651-438-01 59651-438 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20220208 N/A ANDA ANDA214982 Aurobindo Pharma Limited DIGOXIN .25 mg/1 100 TABLET in 1 BOTTLE (59651-438-01)
59651-438-99 59651-438 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20220208 N/A ANDA ANDA214982 Aurobindo Pharma Limited DIGOXIN .25 mg/1 1000 TABLET in 1 BOTTLE (59651-438-99)
59651-436-99 59651-436 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20220208 N/A ANDA ANDA214982 Aurobindo Pharma Limited DIGOXIN .0625 mg/1 1000 TABLET in 1 BOTTLE (59651-436-99)
59651-436-01 59651-436 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20220208 N/A ANDA ANDA214982 Aurobindo Pharma Limited DIGOXIN .0625 mg/1 100 TABLET in 1 BOTTLE (59651-436-01)
50268-238-15 50268-238 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20240711 N/A ANDA ANDA214982 AvPAK DIGOXIN .125 mg/1 50 BLISTER PACK in 1 BOX (50268-238-15) / 1 TABLET in 1 BLISTER PACK (50268-238-11)
59651-437-99 59651-437 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20220208 N/A ANDA ANDA214982 Aurobindo Pharma Limited DIGOXIN .125 mg/1 1000 TABLET in 1 BOTTLE (59651-437-99)
70518-3859-0 70518-3859 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20230911 N/A ANDA ANDA214982 REMEDYREPACK INC. DIGOXIN .125 mg/1 30 TABLET in 1 BLISTER PACK (70518-3859-0)
70518-3860-0 70518-3860 HUMAN PRESCRIPTION DRUG Digoxin Digoxin TABLET ORAL 20230911 N/A ANDA ANDA214982 REMEDYREPACK INC. DIGOXIN .25 mg/1 30 TABLET in 1 BLISTER PACK (70518-3860-0)
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